Quality Assurance Associate
$65k - $85kAmpa
Quality Assurance AssociateAmpa is a pioneering neurotechnology startup developing brain stimulation technology to help eradicate depression. We will improve millions of lives by making this transformative treatment universally accessible. Joining us means you'll be part of a rapidly growing startup with significant equity opportunities and a major impact on our future.What to Expect: Working at Ampa is a rare chance to help transform global mental health and save millions of lives — a level of impact that demands deep commitment. Success here requires resilience, adaptability, and the discipline to put in long hours. If you thrive in a high-intensity, fast-changing environment and want your work to truly matter, you may do the best work of your life here.Role Overview:We're seeking a sharp, detail-oriented Quality Assurance Associate to help us deliver rock-solid, clinic-ready software for our next-generation neuromodulation device. In this role, you'll be responsible for manually testing our Android app, website, and TMS medical device, ensuring every feature is stable, every workflow is seamless, and every bug is caught before it reaches the clinic. You'll test our apps across multiple platforms, confirm interaction with our hardware device, report bugs, and help us ship high-quality builds every day.Tech Stack:Frontend: React, React Native, AndroidBackend: Python, Node.jsDatabase: PostgreSQLCloud: AWS (ECS, CDK, Glue, Firehose, EventBridge)Hardware: Transcranial Magnetic Stimulation (TMS) medical deviceKey Responsibilities:Test the Android app, web platform, and TMS device for functionality, regressions, and overall stabilityManually verify interactions between the app and hardware TMS deviceExecute full QA passes on daily builds across platformsWrite clear, detailed, and reproducible bug reportsRe-test resolved issues and confirm successful fixesMaintain and update lightweight test plans and checklistsIdentify and communicate edge cases, corner conditions, and failure scenarios to the teamWhat We're Looking For:Attention to Detail: You spot inconsistencies and edge cases others missPersistence: You can execute repetitive tests without losing focusClear Communicator: You can write bugs and explain repro steps conciselyCuriosity: You want to understand how the app, hardware, and workflows fit togetherReliability: You take ownership of your work and follow throughExperience: 2-4 years of experience manually testing Android devices and web applications. Experience with automation is a plus.Why Join Ampa?Impact: Lead the development of transformative mental health technologies.Growth: Thrive in a startup environment with rapid innovation.Stability: Enjoy startup benefits with a secure product line.Ownership: Receive substantial equity as an early team member.Logistics:Work Mode: In-personLocation: Palo AltoCompensation: $65,000 - $85,000, plus equityEmployment: Full-time Ampa
$55k - $65k
...work to truly matter, you may do the best work of your life here. Role Overview We’re seeking a sharp, detail-oriented Quality Assurance Associate to help us deliver rock-solid, clinic-ready software for our next-generation neuromodulation device. In this role, you’ll...SuggestedFull timePart time- ...cell-free DNA circulating in the body to assist physicians to make rapid treatment decisions. Position Summary The Quality Assurance Associate is an enthusiastic, self-motivated person with great communication skills. Along with the duties described below, this...SuggestedHourly payPart timeWork at officeLocal areaFlexible hours
$85k - $105k
...top-tier investors. Position Overview: We are seeking a Quality Assurance Specialist to support the day-to-day quality and compliance... ...qualification, maintenance and calibration records, and associated documentation. Coordinate nonconformance reports (NCRs),...SuggestedWork at office- Karius is seeking a part-time Quality Assurance Associate in Redwood City, CA to support the internal quality framework, audits, CAPAs, deviations, and training. This role requires strong writing, organization, and collaboration across teams in a rapidly evolving biotech...SuggestedHourly payPart time
- ...talent to drive their business forward. If you only make one career connection today, connect with Kelly. Job Description Quality Assurance Associate Kelly Services is currently recruiting for Quality Control Data Labeling Associates to help one of our client’s software...SuggestedHourly payFull timeTemporary workImmediate startMonday to Friday
- Karius in Redwood City, CA, seeks a Part-time Quality Assurance Associate to support the internal quality framework, document control, audits, CAPAs, deviations, and related activities. The role is approximately 28 hours per week in a fast-paced biotech startup. You will...Part time
$55k - $65k
...Quality Assurance Inspector The Olander family of companies are a full-line distributor of standard and metric fasteners, including commercial and specialty fasteners, precision hardware, electromechanical components, tools, adhesives, and wire management products....Work at office- ...Quality Assurance Specialist /Auditor LeanTeq is best-in-class in a very niche part of the semiconductor industry and is looking for quality-oriented people who enjoy working in a great culture to join our team. Our company does chemical cleaning of the manufacturing...Work at officeNight shift
- ...& Telemetry Specialist IV Description: ~ We’re looking for a QA Data Analyst & Telemetry Specialist to help drive our product quality efforts through insightful data analysis, robust reporting, and close collaboration with engineering teams. This hybrid role combines...
$120k - $150k
...process improvement projects.Monitor, analyze, and communicate key quality metrics and KPIs related to document lifecycle management and... ...5 years of Pharma/Biotech industry experience in Quality Assurance (QA) in a GxP environment.Experience in developing and implementing...Full timeWork at officeLocal areaWorldwide$89.3k - $146.9k
...Summary: Engages in planned and systematic activities to provide confidence that requirements for quality and quality improvement are being met. The Quality Assurance Specialist recommends revisions to, or creation of, new protocols, policies, procedures and/or systems...Full timeTemporary workWork experience placementInternshipWork at officeWorldwideFlexible hours$71 per hour
...closely with both internal teams and international vendor testers to keep projects on track. If you love the intersection of language, quality, and process, and can stay sharp under tight, fast-moving timelines, this role is built for you. What You'll Do: Coordinate...Full timeContract work- Scorpion Therapeutics is seeking an experienced QA professional to review analytical quality documentation supporting regulatory submissions and batch dispositions. The role emphasizes GMP compliance, method validation oversight, and collaboration with CMOs and laboratories...
- Responsibilities Review and approve analytical quality documentation supporting regulatory submissions (INDs, NDAs, amendments, supplements... ..., method validation protocols/reports, method transfers, and associated change controls. Review specifications, specification...Contract workFlexible hours
- Responsible for test and analysis of issues across Internal and OEM configurations. The role ensures CI/CD quality, compliance with OEM requirements, and readiness towards release. Key Responsibilities Device Setup & Configuration Flash builds onto Yukon boards and OEM...
$105k - $129k
...within our company and in the lives of patients we serve. The Quality Assurance Specialist III, Analytical is responsible for the review and... ...validation protocols and reports, method transfers, and associated change controls Participate in the review of specifications...Full timeContract workWork at officeFlexible hours2 days per week3 days per week- A clinical-stage biotech company is seeking a Senior Specialist in Quality Assurance to oversee compliance and support quality investigation processes. The ideal candidate will have over 4 years of experience in a relevant role within the biotech sector and a Bachelor’s...
- LeanTeq 濂達科技 in Milpitas, California, is seeking a dedicated Quality Assurance Specialist. The role focuses on ensuring compliance with quality standards like ISO 9001:2015 and ISO/IEC 17025:2017, driving process improvements, and conducting audits. Ideal candidates will...
- ...Job Description: As a quality assurance associate, you will be responsible for inspecting materials and packaging to make sure they meet quality requirements. The job involves the completion of daily QA reports and documentation. Role: Inspect and test PCBA prototypes...Temporary workWork experience placementLocal area
$23 per hour
Are you meticulous, technically-minded, and committed to high standards? Become a quality assurance associate with a highly flexible schedule. We offer short-term mandates in high-quality manufacturing and distribution, allowing you to apply your precision inspection skills...Temporary workWork experience placementLocal areaImmediate startFlexible hours$105k - $129k
Ardelyx is seeking a Quality Assurance Specialist III, Analytical to lead review and approval of analytical quality documentation for commercial and clinical products, collaborating with CMOs and internal teams. This hybrid role is based in Newark, CA, requiring 2-3 days...- Protagonist Therapeutics is seeking a Specialist/Sr. Specialist, Quality Assurance to perform GMP QA activities supporting manufacturing. The role reports to the Head of QA and prioritizes QA GMP support with a risk-based approach, including batch record and deviation reviews...Work at office
$105k - $125k
Revance is seeking a Sr. Specialist, Quality Assurance in Newark, CA for hands-on QA within Quality Systems, focusing on lifecycle management of GxP facilities, instruments, and computerized systems, with collaboration across Quality Control, Manufacturing, IT, Supply Chain...Work at office- Guardant Health in Redwood City, CA is seeking a Senior Clinical Laboratory Scientist to perform high complexity molecular testing, including next generation sequencing, and uphold QC/QA standards. This on-site role requires meticulous records and the ability to multi-task...
- ...a Clinical Laboratory Scientist II in Redwood City, CA to perform high-complexity testing (Next generation DNA sequencing), ensure quality control, report patient results, and maintain compliant records. The role requires a California CLS license, a BA/BS in Biomedical...
- Bio-Techne is seeking a Sr. Quality Assurance Specialist to ensure quality processes are compliant with ISO 13485 and FDA QSR. You will lead document control, internal audits, CAPA activities, and regulatory reporting while supporting batch record review and material disposition...
- ...QA AuditorSeeking a QA Auditor to perform the audits, labeling, final packaging inspection and final quality audit for all systems, upgrades and miscellaneous kits prior to shipment.Job Description:Responsible for performing the auditing, labeling, final packaging inspection...Full timeFor contractors
$103.5k - $181k
...shape a healthier, brighter future for all. Learn about the Danaher Business System which makes everything possible. The Senior Quality Assurance Specialist is responsible for serving as the primary on-site Quality representative for IDT's Sunnyvale operations while...Full time$102.09k - $132.11k
...protocols and reports.Maintains accurate, complete, and timely (ALCOA) quality records in accordance with GMP and quality systems.Supports QA... ...Practices (cGMPs).Demonstrates working knowledge of quality assurance systems, methods and procedures.Demonstrates knowledge of FDA /...Full timeFor contractorsWork at officeLocal area- Bio-Techne is seeking a Quality Assurance Specialist to ensure that quality requirements are met and to support continuous improvement. The role involves document control, internal audits, CAPA management, and validation activities to uphold ISO 13485 and FDA Quality System...
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